IP Library Granted Patent US 10,174,127
Granted Patent B2
US 10,174,127 · App. 15/548,919 · Granted Jan 8, 2019

Human neutralizing antibodies binding to influenza neuraminidase

Inventors: Miriam Verena Bujny (The Hague, NL); Remko Van Der Vlugt (Zoetermeer, NL)
Assignee: Janssen Vaccines & Prevention B.V.
C07K16/40C07K16/1018G01N33/56983C07K2317/21C07K2317/33C07K2317/56C07K2317/565C07K2317/732C07K2317/76C07K2317/92G01N2333/924G01N2469/10
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Quick Facts
Patent No.
US 10,174,127
App. No.
15/548,919
Granted
Jan 8, 2019
Kind
B2
Abstract

The present invention provides influenza neuraminidase (NA)-binding human antibodies, which are capable of neutralizing at least one influenza A virus strain comprising NA of the N1 subtype, and antigen-binding fragments thereof. In certain embodiments, the antibodies or antigen-binding fragments furthermore are capable of neutralizing at least one influenza A virus strain comprising NA of the N2 subtype. The invention furthermore relates to the use of said antibodies or antigen-binding fragments in the diagnosis, prophylaxis and/or treatment of influenza infection.

Claims (30)

1. An isolated antibody or antigen-binding fragment thereof that specifically binds neuraminidase (NA) of an influenza A virus, wherein the antibody, or antigen binding fragment is selected from the group consisting of:

a) an antibody, or antigen-binding fragment, comprising a heavy chain CDR1 region of SEQ ID NO: 1, a heavy chain CDR2 region of SEQ ID NO:2, and a heavy chain CDR3 region of SEQ ID NO:3, and a light chain CDR1 region of SEQ ID NO: 13, a light chain CDR2 region of SEQ ID NO: 14, and a light chain CDR3 region of SEQ ID NO: 15;

b) an antibody or antigen-binding fragment comprising a heavy chain CDR1 region of SEQ ID NO:4, a heavy chain CDR2 region of SEQ ID NO:5, and a heavy chain CDR3 region of SEQ ID NO:6, and a light chain CDR1 region of SEQ ID NO: 16, a light chain CDR2 region of SEQ ID NO: 17, and a light chain CDR3 region of SEQ ID NO: 18;

c) an antibody or antigen-binding fragment comprising a heavy chain CDR1 region of SEQ ID NO:7, a heavy chain CDR2 region of SEQ ID NO:8, and a heavy chain CDR3 region of SEQ ID NO:9, and a light chain CDR1 region of SEQ ID NO: 19, a light chain CDR2 region of SEQ ID NO:20, and a light chain CDR3 region of SEQ ID NO:21; and

d) an antibody or antigen-binding fragment comprising a heavy chain CDR1 region of SEQ ID NO: 10, a heavy chain CDR2 region of SEQ ID NO: 11, and a heavy chain CDR3 region of SEQ ID NO: 12, and a light chain CDR1 region of SEQ ID NO:22, a light chain CDR2 region of SEQ ID NO:23, and a light chain CDR3 region of SEQ ID NO:24.

2. The antibody, or antigen-binding fragment thereof, according to claim 1 , which is capable of neutralizing at least one influenza A virus strain comprising NA of the N1 subtype.

3. The antibody, or antigen-binding fragment thereof, according to claim 1 , wherein the antibody or antigen-binding fragment furthermore is capable of neutralizing at least one influenza A virus strain comprising NA of the N2 subtype.

4. The antibody, or antigen-binding fragment thereof, according to claim 1 , wherein the antibody or antigen-binding fragment has neuraminidase inhibiting activity against at least one influenza virus strain comprising NA of the N1 subtype.

5. The antibody, or antigen-binding fragment thereof, according to claim 3 , wherein the antibody or antigen-binding fragment has neuraminidase inhibiting activity against at least one influenza virus strain comprising NA of the N1 subtype and at least one influenza virus strain comprising NA of the N2 subtype.

6. The antibody, or antigen-binding fragment thereof, according to claim 1 , wherein the antibody or antigen-binding fragment has no neuraminidase inhibiting activity.

7. An isolated antibody or antigen-binding fragment thereof that specifically binds neuraminidase (NA) of an influenza A virus, wherein the antibody or antigen binding fragment is selected from the group consisting of:

a) an antibody, or antigen-binding fragment, comprising a heavy chain variable fragment of SEQ ID NO: 25; and a light chain variable region of SEQ ID NO: 26;

b) an antibody, or antigen-binding fragment, comprising a heavy chain variable fragment of SEQ ID NO: 27; and a light chain variable region of SEQ ID NO: 28;

c) an antibody, or antigen-binding fragment, comprising a heavy chain variable fragment of SEQ ID NO: 29; and a light chain variable region of SEQ ID NO: 30; and

d) an antibody, or antigen-binding fragment, comprising a heavy chain variable fragment of SEQ ID NO: 31; and a light chain variable region of SEQ ID NO: 32.

8. A nucleic acid molecule encoding the antibody or antigen-binding fragment according to claim 1 .

9. An immunoconjugate comprising the antibody or antigen-binding fragment according to claim 1 , further comprising a tag.

10. A pharmaceutical composition comprising the immunoconjugate according to claim 9 .

11. A pharmaceutical composition comprising the antibody or antigen-binding fragment according to claim 1 .

12. A pharmaceutical composition comprising the antibody or antigen-binding fragment according to claim 7 .

13. A method of treating or preventing influenza infection in a subject in need thereof, the method comprising administering to the subject the pharmaceutical composition according to claim 10 .

14. A method of treating or preventing influenza infection in a subject in need thereof, the method comprising administering to the subject the pharmaceutical composition according to claim 11 .

15. A method of treating or preventing influenza infection in a subject in need thereof, the method comprising administering to the subject the pharmaceutical composition according to claim 12 .

16. A method of diagnosing influenza infection in a subject, the method comprising contacting a sample from the subject with the antibody or antigen-binding fragment according to claim 1 .

17. A method of diagnosing influenza infection in a subject, the method comprising contacting a sample from the subject with the immunoconjugate according to claim 9 .

18. A method of diagnosing influenza infection in a subject, the method comprising contacting a sample from the subject with the antibody or antigen-binding fragment according to claim 7 .

19. An immunoconjugate comprising the antibody or antigen-binding fragment according to claim 7 , further comprising a tag.

20. A pharmaceutical composition comprising the immunoconjugate according to claim 19 .

21. A method of diagnosing influenza infection in a subject, the method comprising contacting a sample from the subject with the immunoconjugate according to claim 19 .

22. A nucleic acid molecule encoding the antibody or antigen-binding fragment according to claim 7 .

Assignments (2)
CHANGE OF NAME Recorded Aug 10, 2017
From: CRUCELL HOLLAND B.V.
To: JANSSEN VACCINES & PREVENTION B.V.
Reel/Frame 043513/0865 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2017
From: BUJNY, MIRIAM VERENA; VAN DER VLUGT, REMKO
To: CRUCELL HOLLAND B.V.
Reel/Frame 043201/0918 →
Priority Claims (1)
EP 15153891 · Feb 5, 2015 · regional
Continuity (1)
Related Publication 20180016348A1 · Jan 18, 2018
Cited By (1)
US 12,509,503